| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA118898
Max Phase: Preclinical
Molecular Formula: C19H15NO2
Molecular Weight: 289.33
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Oc1ccc(C(=Cc2ccccn2)c2ccc(O)cc2)cc1
Standard InChI: InChI=1S/C19H15NO2/c21-17-8-4-14(5-9-17)19(13-16-3-1-2-12-20-16)15-6-10-18(22)11-7-15/h1-13,21-22H
Standard InChI Key: IDDZZJIJKOUMOD-UHFFFAOYSA-N
Associated Targets(non-human)
Estrogen receptor 420 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 289.33 | Molecular Weight (Monoisotopic): 289.1103 | AlogP: 4.08 | #Rotatable Bonds: 3 |
| Polar Surface Area: 53.35 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.04 | CX Basic pKa: 4.50 | CX LogP: 4.16 | CX LogD: 4.14 |
| Aromatic Rings: 3 | Heavy Atoms: 22 | QED Weighted: 0.76 | Np Likeness Score: -0.25 |
References
| 1. Meyers MJ, Carlson KE, Katzenellenbogen JA.. (1998) Facile synthesis of high affinity styrylpyridine systems as inherently fluorescent ligands for the estrogen receptor., 8 (24): [PMID:9934476] [10.1016/s0960-894x(98)00652-0] |
Source
Source(1):